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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Class Implantable

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CoRoent - 00887517311399

CoRoent XLW Ti, 14x22x60mm 10°
Nuvasive, Inc.
6421460
In Commercial Distribution

  • 00887517311399 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517311375

CoRoent XLW Ti, 14x22x50mm 10°
Nuvasive, Inc.
6421450
In Commercial Distribution

  • 00887517311375 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517311368

CoRoent XLW Ti, 14x22x45mm 10°
Nuvasive, Inc.
6421445
In Commercial Distribution

  • 00887517311368 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517311337

CoRoent® XLW Ti, 12x22x55mm 10°
Nuvasive, Inc.
6421255
In Commercial Distribution

  • 00887517311337 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517311306

CoRoent® XLW Ti, 12x22x40mm 10°
Nuvasive, Inc.
6421240
In Commercial Distribution

  • 00887517311306 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310972

CoRoent® XLW Ti, 10x22x50mm 10°
Nuvasive, Inc.
6421050
In Commercial Distribution

  • 00887517310972 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310941

CoRoent® XLW Ti, 8x22x60mm 10°
Nuvasive, Inc.
6420860
In Commercial Distribution

  • 00887517310941 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310927

CoRoent® XLW Ti, 8x22x50mm 10°
Nuvasive, Inc.
6420850
In Commercial Distribution

  • 00887517310927 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310910

CoRoent® XLW Ti, 8x22x45mm 10°
Nuvasive, Inc.
6420845
In Commercial Distribution

  • 00887517310910 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310590

CoRoent® XLW Ti, 16x22x60mm
Nuvasive, Inc.
6416260
In Commercial Distribution

  • 00887517310590 ()


  • Polymeric spinal interbody fusion cage
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